Epitope-focused immunogens targeting the hepatitis C virus glycoproteins induce broadly neutralizing antibodies

被引:0
|
作者
Nagarathinam, Kumar [1 ,16 ]
Scheck, Andreas [2 ,3 ,16 ]
Labuhn, Maurice [4 ]
Stroeh, Luisa J. [5 ]
Herold, Elisabeth [1 ]
Veselkova, Barbora [1 ]
Tune, Sarah [6 ,7 ]
Cramer, Johannes T. [5 ]
Rosset, Stephane [2 ,3 ]
Vollers, Sabrina S. [2 ,3 ,17 ]
Bankwitz, Dorothea [4 ]
Ballmaier, Matthias [8 ]
Boening, Heike [5 ]
Roth, Edith [9 ]
Khera, Tanvi [4 ]
Ahsendorf-Abidi, Henrike P. [5 ]
Dittrich-Breiholz, Oliver [10 ]
Obleser, Jonas [6 ,7 ]
Nassal, Michael [11 ]
Jaeck, Hans-Martin [9 ]
Pietschmann, Thomas [4 ,12 ,13 ]
Correia, Bruno E. [2 ,3 ]
Krey, Thomas [1 ,5 ,13 ,14 ,15 ]
机构
[1] Univ Lubeck, Inst Biochem, Ctr Struct & Cell Biol Med, D-23562 Lubeck, Germany
[2] Ecole Polytech Fed Lausanne, Inst Bioengn, CH-1015 Lausanne, Switzerland
[3] Swiss Inst Bioinformat SIB, CH-1015 Lausanne, Switzerland
[4] Joint Venture Helmholtz Ctr Infect Res & Hannover, Ctr Expt & Clin Infect Res, TWINCORE, Inst Expt Virol, D-30625 Hannover, Germany
[5] Hannover Med Sch, Inst Virol, DE-30625 Hannover, Germany
[6] Univ Lubeck, Dept Psychol, D-23562 Lubeck, Germany
[7] Univ Lubeck, Ctr Brain Behav & Metab, D-23562 Lubeck, Germany
[8] Hannover Med Sch, Cent Res Facil Cell Sorting, D-30625 Hannover, Germany
[9] Friedrich Alexander Univ Erlangen Nurnberg, Dept Internal Med 3, Div Mol Immunol, D-91054 Erlangen, Germany
[10] Hannover Med Sch, Res Core Unit Genom, D-30625 Hannover, Germany
[11] Univ Hosp Freiburg, Dept Internal Med Mol Biol 2, D-79106 Freiburg, Germany
[12] German Ctr Infect Res DZIF, Partner Site Hannover Braunschweig, D-30625 Hannover, Germany
[13] Hannover Med Sch, Excellence Cluster RESIST 2155, D-30625 Hannover, Germany
[14] German Ctr Infect Res DZIF, Partner Site Hamburg Lubeck Borstel Riems, D-38124 Braunschweig, Germany
[15] Ctr Struct Syst Biol CSSB, D-22607 Hamburg, Germany
[16] Ridgeline Discovery Gmbh, CH-4057 Basel, Switzerland
[17] Ichnos Sci SA, CH-2300 La Chaux de Fonds, Switzerland
来源
SCIENCE ADVANCES | 2024年 / 10卷 / 49期
关键词
E2; GLYCOPROTEIN; STRUCTURAL BASIS; MONOCLONAL-ANTIBODIES; BINDING DOMAIN; VACCINE; DESIGN; COMPLEX; SITE; FLEXIBILITY; PARTICLES;
D O I
10.1126/sciadv.ado2600
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Hepatitis C virus (HCV) infection causes similar to 290,000 annual human deaths despite the highly effective antiviral treatment available. Several viral immune evasion mechanisms have hampered the development of an effective vaccine against HCV, among them the remarkable conformational flexibility within neutralization epitopes in the HCV antigens. Here, we report the design of epitope-focused immunogens displaying two distinct HCV cross-neutralization epitopes. We show that these immunogens induce a pronounced, broadly neutralizing antibody response in laboratory and transgenic human antibody mice. Monoclonal human antibodies isolated from immunized human antibody mice specifically recognized the grafted epitopes and neutralized four diverse HCV strains. Our results highlight a promising strategy for developing HCV immunogens and provide an encouraging paradigm for targeting structurally flexible epitopes to improve the induction of neutralizing antibodies.
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页数:15
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